rs5030656
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 2 | CYP2D6*9 homozygote |
(-;AAG) | 2 | carrier of one CYP2D6*9 allele |
(AAG;AAG) | 0 | normal |
Reference | GRCh38 38.1/142 |
Chromosome | 22 |
Position | 42128174 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs5030656 |
dbSNP (classic) | rs5030656 |
ClinGen | rs5030656 |
ebi | rs5030656 |
HLI | rs5030656 |
Exac | rs5030656 |
Gnomad | rs5030656 |
Varsome | rs5030656 |
LitVar | rs5030656 |
Map | rs5030656 |
PheGenI | rs5030656 |
Biobank | rs5030656 |
1000 genomes | rs5030656 |
hgdp | rs5030656 |
ensembl | rs5030656 |
geneview | rs5030656 |
scholar | rs5030656 |
rs5030656 | |
pharmgkb | rs5030656 |
gwascentral | rs5030656 |
openSNP | rs5030656 |
23andMe | rs5030656 |
SNPshot | rs5030656 |
SNPdbe | rs5030656 |
MSV3d | rs5030656 |
GWAS Ctlg | rs5030656 |
GMAF | 0.01148 |
Max Magnitude | 2 |
rs5030656, also known as 2615_2617delAAG or K281del, is a SNP in the CYP2D6 gene.
The rs5030656(-) allele defines the CYP2D6*9 variant, which has decreased activity.
[PMID 23133420] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.